ChemicalBook--->CAS DataBase List--->2538-61-6

2538-61-6

2538-61-6 Structure

2538-61-6 Structure
IdentificationMore
[Name]

(2,6-DIMETHYL-PHENYL)-HYDRAZINE
[CAS]

2538-61-6
[Synonyms]

TIMTEC-BB SBB001780
DimethylphenylhydrazineHCl
[Molecular Formula]

C8H12N2
[MDL Number]

MFCD02656464
[Molecular Weight]

136.19
[MOL File]

2538-61-6.mol
Chemical PropertiesBack Directory
[Melting point ]

210-211 °C
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

Off-white to light yellow Solid
[CAS DataBase Reference]

2538-61-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2928009090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2,6-Dimethylaniline-->Benzenediazonium, 2,6-dimethyl-, chloride (1:1)-->Stannous chloride-->Hydrochloric acid
Hazard InformationBack Directory
[Uses]

2,6-Dimethylphenylhydrazine Hydrochloride is used as a reagent in the synthesis of 3-arylimino-2,3,5,6-tetrahydro-4H-1,4-thiazines and related cyclic amidines which exhibit potential antihypertensive activity.
[Synthesis]

Benzenediazonium, 2,6-dimethyl-, chloride (1:1)

85518-80-5

(2,6-DIMETHYL-PHENYL)-HYDRAZINE

2538-61-6

Under stirring conditions, 2,6-dimethylaniline (5.0 g, 41.3 mmol) was dissolved in 50% aqueous HCl solution (45 mL) and cooled to 0°C. At the same temperature, NaNO2 solution (2.85 g, 41.3 mmol dissolved in 22.5 mL of water) was slowly added. The temperature was strictly controlled not to exceed 5 °C during addition. After addition, the resulting bright orange diazonium salt solution was continued to be stirred at 0 °C for 20 min. Subsequently, a pre-cooled (0 °C) solution of SnCl2 (11.0 g, 57.8 mmol) in concentrated HCl (30 mL) was added to the reaction mixture over 5 min. The reaction mixture was gradually warmed to room temperature with continuous stirring for 6 hours. Upon completion of the reaction, the precipitate was collected by filtration, washed with a little cold water and dried under vacuum to afford (2,6-dimethylphenyl)hydrazine hydrochloride as a white amorphous solid (7.00 g, 98% yield). The product was detected by ES-MS showing m/z 137.0 (MH+) and HPLC retention time of 1.09 min, which can be directly used in the subsequent reaction without further purification.

[References]

[1] Patent: US2005/192294, 2005, A1. Location in patent: Page/Page column 10
Spectrum DetailBack Directory
[Spectrum Detail]

(2,6-DIMETHYL-PHENYL)-HYDRAZINE(2538-61-6)1HNMR
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